A Novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypes-Reference-Cited by-同舟云学术

A Novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypes

Published:2014-04 Issue: Volume:64 Page:131-141
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Johnston Ann J.,Kang Jing-Qiong,Shen Wangzhen,Pickrell William O.,Cushion Thomas D.,Davies Jeffrey S.,Baer Kristin,Mullins Jonathan G.L.,Hammond Carrie L.,Chung Seo-Kyung,Thomas Rhys H.,White Cathy,Smith Phil E.M.,Macdonald Robert L.,Rees Mark I.

Funder

National Institute of Social Care and Health Research (NISCHR)

Waterloo Foundation to MIR, Epilepsy Research UK (ERUK) Fellowship

CURE

National Institute of Health

National Institutes of Health

Publisher

Elsevier BV

Subject

Neurology

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